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MEIKIN meiotic kinetochore factor [ Homo sapiens (human) ]

Gene ID: 728637, updated on 17-Jun-2019

Summary

Official Symbol
MEIKINprovided by HGNC
Official Full Name
meiotic kinetochore factorprovided by HGNC
Primary source
HGNC:HGNC:51253
See related
Ensembl:ENSG00000239642 MIM:616232
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Restricted expression toward testis (RPKM 3.3) See more
Orthologs

Genomic context

See MEIKIN in Genome Data Viewer
Location:
5q31.1
Exon count:
13
Annotation release Status Assembly Chr Location
109.20190607 current GRCh38.p13 (GCF_000001405.39) 5 NC_000005.10 (131806990..131945663, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (131142683..131281391, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene Rap guanine nucleotide exchange factor 6 Neighboring gene folliculin interacting protein 1 Neighboring gene ACTB pseudogene 4 Neighboring gene uncharacterized LOC101927693 Neighboring gene acyl-CoA synthetase long chain family member 6 Neighboring gene uncharacterized LOC105379174 Neighboring gene interleukin 3

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Markers

Potential readthrough

Included gene: ACSL6

Homology

Gene Ontology Provided by GOA

Process Evidence Code Pubs
female meiosis chromosome segregation IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
female meiosis chromosome segregation ISS
Inferred from Sequence or Structural Similarity
more info
 
homologous chromosome segregation IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
homologous chromosome segregation ISS
Inferred from Sequence or Structural Similarity
more info
 
male meiosis chromosome segregation IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
male meiosis chromosome segregation ISS
Inferred from Sequence or Structural Similarity
more info
 
meiotic sister chromatid cohesion involved in meiosis I IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
meiotic sister chromatid cohesion involved in meiosis I ISS
Inferred from Sequence or Structural Similarity
more info
 
meiotic sister chromatid cohesion, centromeric IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
meiotic sister chromatid cohesion, centromeric ISS
Inferred from Sequence or Structural Similarity
more info
 
Component Evidence Code Pubs
condensed chromosome kinetochore IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
condensed chromosome kinetochore ISS
Inferred from Sequence or Structural Similarity
more info
 
condensed nuclear chromosome, centromeric region IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
condensed nuclear chromosome, centromeric region ISS
Inferred from Sequence or Structural Similarity
more info
 

General protein information

Preferred Names
meiosis-specific kinetochore protein

NCBI Reference Sequences (RefSeq)

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001303622.2NP_001290551.1  meiosis-specific kinetochore protein

    See identical proteins and their annotated locations for NP_001290551.1

    Status: VALIDATED

    Source sequence(s)
    AB987829, BG181951, DB455285
    Consensus CDS
    CCDS75292.2
    UniProtKB/Swiss-Prot
    A0A087WXM9
    Related
    ENSP00000488568.1, ENST00000442687.6

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000005.10 Reference GRCh38.p13 Primary Assembly

    Range
    131806990..131945663 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001278059.1: Suppressed sequence

    Description
    NM_001278059.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript and the protein.
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